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D058070: Asymptomatic Diseases

Developed by Shray Alag, The Harker School
Sections: Correlations, Clinical Trials, and HPO

Correlations computed by analyzing all clinical trials.

Navigate: Clinical Trials and HPO


Correlated Drug Terms (13)


Name (Synonyms) Correlation
drug518 Bromhexine 8 MG Wiki 0.50
drug3373 To assess for development of IgG antibodies against SARS-CoV2 Wiki 0.50
drug517 Brief informational infographic Wiki 0.50
Name (Synonyms) Correlation
drug2744 Rapid Antigen Test Wiki 0.50
drug2492 Placebo control (non-behavioral infographic) Wiki 0.50
drug531 Butterfly iQ Wiki 0.50
drug525 Bucillamine Wiki 0.35
drug1371 Guduchi Ghan Vati Wiki 0.35
drug1503 Hydroxychloroquine Sulfate Regular dose Wiki 0.35
drug1502 Hydroxychloroquine Sulfate Loading Dose Wiki 0.35
drug739 Chloroquine Wiki 0.20
drug1492 Hydroxychloroquine Sulfate Wiki 0.14
drug2448 Placebo Wiki 0.05

Correlated MeSH Terms (7)


Name (Synonyms) Correlation
D003333 Coronaviridae Infections NIH 0.22
D012327 RNA Virus Infections NIH 0.18
D014777 Virus Diseases NIH 0.05
Name (Synonyms) Correlation
D045169 Severe Acute Respiratory Syndrome NIH 0.04
D003141 Communicable Diseases NIH 0.04
D018352 Coronavirus Infections NIH 0.04
D007239 Infection NIH 0.02

Correlated HPO Terms (0)


Name (Synonyms) Correlation

Clinical Trials

Navigate: Correlations   HPO

There are 4 clinical trials


1 Use and Dosage of Hydroxychloroquine and Chloroquine to Convert Real Time Polymerase Chain Reaction (RT-PCR) Positive Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Coronavirus Infectious Disease 2019 (COVID-19) Patients to RT- PCR-Negative as a Means to Reduce Hospitalization Rate

To create a protocol for treatment of Pakistani patients with SARS-CoV-2 infection with an intent to reduce burden on institutional healthcare services by determining efficacy of different quinone drug dosing regimens in controlling SARS-CoV-2 infection for asymptomatic patients.

NCT04346667
Conditions
  1. SARS-CoV-2
  2. Coronavirus Infection
  3. Asymptomatic Condition
  4. COVID-19
Interventions
  1. Drug: Hydroxychloroquine Sulfate Regular dose
  2. Drug: Hydroxychloroquine Sulfate Loading Dose
  3. Drug: Chloroquine
  4. Drug: Placebo
MeSH:Coronavirus Infections Severe Acute Respiratory Syndrome Asymptomatic Diseases

Primary Outcomes

Description: Percentage of patients who become RT-PCR negative with two RT-PCR tests performed at day 6 and day 7

Measure: RT-PCR negative status

Time: 6-7 days

Secondary Outcomes

Description: Time to progression to next stage of SARS-CoV-2 disease severity index

Measure: Progression of symptoms

Time: 7 days

Description: Time to onset of fever (temperature greater than 100 degree F), cough, or shortness of breath (respiratory rate >22 per minute).

Measure: Development of Symptoms

Time: 7 days

Description: Drug related adverse events as determined by data safety and monitoring board (DSMB)

Measure: Adverse events

Time: 7 days
2 ScreenNC: A Study to Determine the Number of Asymptomatic Individuals Who Have Antibodies to the SARS-CoV-2 Infection

Purpose: To determine the number of asymptomatic individuals who have antibodies to SARS-CoV-2, the virus which causes COVID-19

NCT04367740
Conditions
  1. Asymptomatic Condition
  2. Infection Viral
  3. Coronavirus Infections
  4. Severe Acute Respiratory Syndrome Coronavirus 2
  5. Coronaviridae Infections
  6. RNA Virus Infections
  7. Virus Diseases
  8. Communicable Disease
Interventions
  1. Diagnostic Test: To assess for development of IgG antibodies against SARS-CoV2
MeSH:Infection Communicable Diseases Virus Diseases Coronavirus Infections Severe Acute Respiratory Syndrome RNA Virus Infections Coronaviridae Infections Asymptomatic Diseases

Primary Outcomes

Description: Presence or absence of IgG antibodies to SARS-CoV2

Measure: Percentage of Asymptomatic patients with an IgG response from SARS-CoV-2 infection.

Time: at enrollment

Secondary Outcomes

Description: swab for presence of SARS-CoV-2 virus

Measure: Percentage of Asymptomatic patients with viral presence of SARS-CoV-2 infection.

Time: at enrollment
3 A Retrospective Study on Efficacy and Safety of Guduchi Ghan Vati for Covid-19 Asymptomatic Patients

Coronavirus disease 2019 (Covid-19) has been declared global emergency with immediate safety, preventative and curative measures to control the spread of virus. Confirmed cases are treated with clinical management as they are diagnosed but so far, there is no effective treatment or vaccine yet for Covid-19. With recommended guidelines of AYUSH Ministry, India, the use of Ayurveda for Covid-19 has increased; however, its efficacy and safety in Covid-19 confirmed patients remain unclear. Present study examined the efficacy and safety of one of the recommended Ayurveda drug (Guduchi Ghan Vati) compared with standard care for patients with asymptomatic Covid-19 patients.

NCT04480398
Conditions
  1. Covid19
  2. Asymptomatic Condition
Interventions
  1. Drug: Guduchi Ghan Vati
MeSH:Asymptomatic Diseases

Primary Outcomes

Description: Virologic clearance indicates the duration from the first Covid-19 positive result to the first Covid-19 negative result

Measure: Virologic clearance

Time: 21 days

Secondary Outcomes

Description: change in the number of patients going from asymptomatic to moderately disease

Measure: Change in the number of patients going from asymptomatic to moderately disease

Time: 10-days of hospital admission

Description: Total duration of stay in hospital for complete recovery

Measure: Hospital Stay

Time: 21 days

Description: Clinically relevant adverse effects of Guduchi Ghan Vati (Disability, Discomfort reported)

Measure: Clinically relevant adverse effects

Time: 21-days
4 An Approach to Screening for SARS-CoV-2 at YVR: UBC-PHC-WestJet-YVR COVID-19 Screening Study

The primary objective of this pilot study is to determine the feasibility and effectiveness of a COVID-19 screening program for passengers departing from YVR. This research study is conducted by The University of British Columbia (UBC) and Providence Health Care, sponsored by WestJet and Vancouver Airport Authority. The experimental study investigates point-of-care rapid test device for detecting SARS-CoV-2, the virus responsible for COVID-19. The study is investigating a method of rapid-testing for COVID-19 and will help inform the safest and most efficient way of testing departing passengers prior to security screening at Vancouver International Airport (YVR). This study is also evaluating a new passenger management system.

NCT04665193
Conditions
  1. Asymptomatic Condition
  2. Healthy
Interventions
  1. Diagnostic Test: Rapid Antigen Test
MeSH:Asymptomatic Diseases

Primary Outcomes

Description: positive or negative screening result

Measure: COVID-19 status

Time: 15 min

HPO Nodes


HPO

Alphabetical listing of all HPO terms. Navigate: Correlations   Clinical Trials


HPO Nodes


Reports

Data processed on December 13, 2020.

An HTML report was created for each of the unique drugs, MeSH, and HPO terms associated with COVID-19 clinical trials. Each report contains a list of either the drug, the MeSH terms, or the HPO terms. All of the terms in a category are displayed on the left-hand side of the report to enable easy navigation, and the reports contain a list of correlated drugs, MeSH, and HPO terms. Further, all reports contain the details of the clinical trials in which the term is referenced. Every clinical trial report shows the mapped HPO and MeSH terms, which are also hyperlinked. Related HPO terms, with their associated genes, protein mutations, and SNPs are also referenced in the report.

Drug Reports   MeSH Reports   HPO Reports  

Interventions

4,818 reports on interventions/drugs

MeSH

706 reports on MeSH terms

HPO

306 reports on HPO terms

All Terms

Alphabetical index of all Terms

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Python example via Google Colab Notebook